Memory Loss Can Be Now Fully Restored By This New Treatment
Amyloid plaques sit between the neurons and end up as dense
clusters of beta-amyloid molecules, a sticky type of protein that
clumps together and forms these plaques.
There is no vaccine or curbing measure for Alzheimer’s
which affects 50 million people worldwide but researchers and
scientists have been continuously in search of something which could
bring the disease onto a curable front, starting with how to clear the
build-up of defective beta-amyloid and tau proteins from a patient’s
brain. ‘Now a team from the Queensland Brain Institute (QBI) at the
University of Queensland have come up with a pretty promising solution
for removing the former’, the sciencealert.com reported.
In a report published in the Science Translational Medicine
, the team describes the technique as using a particular type of
ultrasound called a focused therapeutic ultrasound, which non-invasively
beams sound waves into the brain tissue.
By oscillating super-fast,
these sound waves are able to gently open up the blood-brain barrier,
which is a layer that protects the brain against bacteria, and stimulate
the brain’s microglial cells to activate. Microglila cells are
basically waste-removal cells, so they’re able to clear out the toxic
beta-amyloid clumps that are responsible for the worst symptoms of
Alzheimer’s.
If the experiment does come out to be a success
then it would be a relief to the millions of people worldwide who are
suffering from the disease.
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The team reports fully restoring the memory function of 75
percent of the mice they tested it on, with zero damage to the
surrounding brain tissue. They found that the treated mice displayed
improved performance in three memory tasks – a maze, a test to get them
to recognise new objects, and one to get them to remember the places
they should avoid.
“We’re extremely excited by this innovation of treating
Alzheimer’s without using drug therapeutics,” one of the team, Jürgen
Götz, said in a press release . “The word ‘breakthrough’ is often
misused, but in this case I think this really does fundamentally change
our understanding of how to treat this disease, and I foresee a great
future for this approach.”
The team further said that they’re planning to experiment with higher animal models first and then turn to humans in 2017.
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